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Association of STAM with rheumatoid arthritis in the Korean populationopen access

Authors
Lee, Hye SoonRemmers, Elaine FLe, Julie M.Kastner, Daniel L.Bae, Sang CheolGregersen, Peter K.
Issue Date
Sep-2007
Publisher
SPRINGER
Citation
MOLECULAR MEDICINE, v.13, no.9-10, pp.455 - 460
Indexed
SCIE
SCOPUS
Journal Title
MOLECULAR MEDICINE
Volume
13
Number
9-10
Start Page
455
End Page
460
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/179637
DOI
10.2119/2007-00072.Lee
ISSN
1076-1551
Abstract
A recent study in the North American White population has documented the association of a common STAT4 haplotype (tagged by rs7574865) with risk for rheumatoid arthritis (RA) and systemic lupus erythematosus. To replicate this finding in the Korean population, we performed a case-control association study. We genotyped 67 single nucleotide polymorphisms (SNPs) within the STAT1 and STAT4 regions in 1123 Korean patients with RA and 1008 ethnicity-matched controls. The most significant four risk SNPs (rs] 1889341, rs7574865, rs8179673, and rs10181656 located within the third intron of STAT4) among 67 SNPs are identical with those in the North American study. All four SNPs have modest risk for RA susceptibility (odds ratio 1.21-1.27). A common haplotype defined by these markers (TTCG) carries significant risk for RA in Koreans (34 percent versus 28 percent, P = 0.0027, OR (95 percent CI) = 1.33 (1.10-1.60)). By logistic regression analysis, this haplotype is an independent risk factor in addition to the classical shared epitope alleles at the HLA-DRB1 locus. There were no significant associations with age of disease onset, radiographic progression, or serologic status using either allelic or haplotypic analysis. Unlike several other risk genes for RA such as PTPN22, PAD14, and FCRL3, a haplotype of the STAT4 gene shows consistent association with RA susceptibility across Whites and Asians, suggesting that this risk haplotype predates the divergence of the major racial groups.
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